[1例产粘蛋白尿路上皮型前列腺腺癌(mpuap),全膀胱切除术后长期存活]。

Q4 Medicine Japanese Journal of Urology Pub Date : 2020-01-01 DOI:10.5980/jpnjurol.111.154
Yusuke Fukiage, Takafumi Kabuto, Ryusei Yokokawa, Manabu Kurosawa
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引用次数: 0

摘要

摘要分泌黏液蛋白的尿路上皮型前列腺腺癌是一种非常罕见的疾病。据报道,MPUAP的进展速度比正常前列腺癌的进展速度要快。我们报告一例长期存活的MPUAP。患者为65岁男性。计算机断层扫描和磁共振成像显示一个囊性病变从前列腺延伸到尿道。经直肠前列腺活检及经尿道肿瘤切除术,病理诊断为腺癌。随后,我们进行了全膀胱切除术、输尿管造口术和盆腔淋巴结切除术。根据病理和免疫染色结果(前列腺特异性抗原阴性、CDX-2阳性、细胞角蛋白20阳性、34β-E12阳性),诊断为MPUAP。术后4年未见复发或转移。
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[A CASE OF MUCIN-PRODUCING UROTHELIAL-TYPE ADENOCARCINOMA OF THE PROSTATE (MPUAP) WITH LONG-TERM SURVIVAL AFTER TOTAL CYSTECTOMY].

Mucin-producing urothelial-type adenocarcinoma of the prostate (MPUAP) is a very rare disease. MPUAP has been reported to progress faster than the rate at which normal prostate cancer progresses. We report a case of MPUAP with long-term survival. The patient was a 65-year-old man. Computed tomography and magnetic resonance imaging showed a cystic lesion extending from the prostate to the urethra. We performed transrectal prostate biopsy and transurethral resection of the tumor, and the pathological diagnosis was adenocarcinoma. Subsequently, we performed total cystectomy, ureterostomy, and pelvic lymphadenectomy. Based on the pathological and immunostaining findings (prostate-specific antigen negativity, CDX-2 positivity, cytokeratin 20 positivity, 34β-E12 positivity), the patient was diagnosed with MPUAP. Four years after the surgery, recurrence or metastasis was not observed.

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来源期刊
Japanese Journal of Urology
Japanese Journal of Urology Medicine-Urology
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0.20
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